has characteristic has characteristic congenital nervous system disorder hypopituitarism combined pituitary hormone deficiencies, genetic form https://rarediseases.info.nih.gov/diseases/2252/familial-hypopituitarism https://www.malacards.org/card/combined_pituitary_hormone_deficiency UMLS:C4273747 pituitary hormone deficiency, combined OMIMPS:613038 multiple pituitary hormone deficiencies, genetic forms GARD:0010602 MEDGEN:906592 Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. Orphanet:95494 genetic hypopituitarism SCTID:718182008 familial hypopituitarism MONDO:0013099 familial congenital hypopituitarism congenital hypogonadotropic hypogonadism inherited hereditary neurological disease